تفاعل #218956

ord-7e2db2a550744864affa141c23fdb9ff

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةA cooled
  2. 2
    أخرىThe cooling bath was then removed
  3. 3
    غسيلwashed several times with water and finally aqueous 5% sodium hydrogen carbonate solution
  4. 4
    أخرىAfter drying
  5. 5
    ترشيح(sodium sulphate), filtration and evaporation the oily residue
  6. 6
    workup.DISSOLUTIONwas re-dissolved in a small volume of a solvent mixture
  7. 7
    غسيلElution of the column
  8. 8
    أخرىwith the same solvent mixture, collection of the appropriate fractions, and evaporation of the combined fractions

الإجراء التجريبي

A cooled (4° C.) mixture of pent-4-enoic acid, isobutyl chloroformate, and triethylamine (each 5.84 mmol) in 10 ml of dichloromethane was stirred 5 hrs under an atmosphere of dry nitrogen gas. The cooling bath was then removed and both triethylamine (1.46 mmol) and 2-(3-diisopropylamino-1-phenyl-propyl)-4-hydroxymethylphenol (1.46 mmol) were added in one portion. After 18 hrs the mixture was diluted with dichloromethane (30 ml), washed several times with water and finally aqueous 5% sodium hydrogen carbonate solution. After drying (sodium sulphate), filtration and evaporation the oily residue was re-dissolved in a small volume of a solvent mixture consisting of ethyl acetate/heptane/triethylamine (65/30/5, vol.-%) and applied on a silica gel flash chromatography column. Elution of the column with the same solvent mixture, collection of the appropriate fractions, and evaporation of the combined fractions gave (±)-pent-4-enoic acid 2-(3-diisopropylamino-1-phenylpropyl)-4-(pent-4-enoyloxymethyl)-phenyl ester as a pale yellow syrupy oil (50% yield), tlc: (4) 0.75. NMR (CDCl3): 18.95, 20.77, 27.75, 28.87, 33.58, 36.83, 42.13, 43.72, 48.71, 65.85, 70.55, 115.47, 115.99, 122.45, 126.26, 127.08, 127.96, 128.11, 28.83, 133.73, 136.38, 136.79, 137.04, 143.77, 148.46, 171.11, 172.78.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07384980B2uspto-grants-2008_06